膦与乙炔的反应。十四。同分异构体:由三芳基膦和二甲基乙酰二羧酸酯合成的2加合物。一个cyclopentenylidenephosphorane

N. Waite, J. Tebby, R. Ward, M. Shaw, Dudley H. Williams
{"title":"膦与乙炔的反应。十四。同分异构体:由三芳基膦和二甲基乙酰二羧酸酯合成的2加合物。一个cyclopentenylidenephosphorane","authors":"N. Waite, J. Tebby, R. Ward, M. Shaw, Dudley H. Williams","doi":"10.1039/J39710001620","DOIUrl":null,"url":null,"abstract":"The reaction of triphenylphosphine and an excess of dimethyl acetylenedicarboxylate gives in addition to the 2H-phosph(V)ole (1), a second product—the cyclopentenylidenephosphorane (2). Reduction of (2) to the dihydro-compound (7) followed by base-catalysed elimination of methanol, gives the cyclopentadienylidenephosphorane (8). The i.r., u.v., n.m.r., and mass spectra of these compounds are discussed.","PeriodicalId":17245,"journal":{"name":"Journal of The Chemical Society C: Organic","volume":"10 1","pages":"1620-1622"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"9","resultStr":"{\"title\":\"Reactions of phosphines with acetylenes. Part XIV. Isomeric 1 : 2 adducts from triarylphosphines and dimethyl acetylenedicarboxylate. A cyclopentenylidenephosphorane\",\"authors\":\"N. Waite, J. Tebby, R. Ward, M. Shaw, Dudley H. Williams\",\"doi\":\"10.1039/J39710001620\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The reaction of triphenylphosphine and an excess of dimethyl acetylenedicarboxylate gives in addition to the 2H-phosph(V)ole (1), a second product—the cyclopentenylidenephosphorane (2). Reduction of (2) to the dihydro-compound (7) followed by base-catalysed elimination of methanol, gives the cyclopentadienylidenephosphorane (8). The i.r., u.v., n.m.r., and mass spectra of these compounds are discussed.\",\"PeriodicalId\":17245,\"journal\":{\"name\":\"Journal of The Chemical Society C: Organic\",\"volume\":\"10 1\",\"pages\":\"1620-1622\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society C: Organic\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/J39710001620\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society C: Organic","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/J39710001620","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 9

摘要

三苯基膦与过量的二甲基乙炔二羧酸盐反应,除生成2h -磷酸(V)孔(1)外,还生成第二个产物——环戊二烯二磷酸(2)。将(2)还原为二氢化合物(7),然后碱催化甲醇消除,生成环戊二烯二磷酸(8)。讨论了这些化合物的红外、紫外、新核磁共振和质谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reactions of phosphines with acetylenes. Part XIV. Isomeric 1 : 2 adducts from triarylphosphines and dimethyl acetylenedicarboxylate. A cyclopentenylidenephosphorane
The reaction of triphenylphosphine and an excess of dimethyl acetylenedicarboxylate gives in addition to the 2H-phosph(V)ole (1), a second product—the cyclopentenylidenephosphorane (2). Reduction of (2) to the dihydro-compound (7) followed by base-catalysed elimination of methanol, gives the cyclopentadienylidenephosphorane (8). The i.r., u.v., n.m.r., and mass spectra of these compounds are discussed.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信